Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.14716757C= , CM000667.2:g.14716757C= | GRCh38 |
| NC_000005.9:g.14716866C= , CM000667.1:g.14716866C= | GRCh37 |
| NC_000005.8:g.14769866C= | NCBI36 |
| NG_008273.1:g.160022G= | |
| NG_008273.2:g.160029G= | |
| NG_051625.1:g.60964C= |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000284268.8:c.1090G= MANE Select | ENSP00000284268.6:p.Ala364= | |
| ENST00000284268.6:c.1090G= | ENSP00000284268.6:p.Ala364= | |
| ENST00000502585.1:n.332G= | ||
| NM_054027.4:c.1090G= | NP_473368.1:p.Ala364= | |
| NM_054027.5:c.1090G= | NP_473368.1:p.Ala364= | |
| XM_017009644.2:c.1006G= | XP_016865133.1:p.Ala336= | |
| NM_054027.6:c.1090G= MANE Select | NP_473368.1:p.Ala364= |